Canonical Allele Identifier: CA1777240077

Gene: PLPBP

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37772879C= , CM000670.2:g.37772879C=	GRCh38
NC_000008.10:g.37630397C= , CM000670.1:g.37630397C=	GRCh37
NC_000008.9:g.37749555C=	NCBI36
NG_053030.1:g.16127C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.444C= MANE Select	ENSP00000333551.3:p.Ser148=
ENST00000328195.7:c.444C=	ENSP00000333551.3:p.Ser148=
ENST00000521631.1:n.127C=
ENST00000523187.5:c.288C=	ENSP00000427886.1:p.Ser96=
ENST00000523358.5:c.444C=	ENSP00000427778.1:p.Ser148=
ENST00000523521.1:c.201C=	ENSP00000429425.1:p.Ser67=
NM_007198.3:c.444C=	NP_009129.1:p.Ser148=
NM_001349346.1:c.444C=	NP_001336275.1:p.Ser148=
NM_001349347.1:c.438C=	NP_001336276.1:p.Ser146=
NM_001349348.1:c.288C=	NP_001336277.1:p.Ser96=
NM_007198.4:c.444C= MANE Select	NP_009129.1:p.Ser148=
NM_001349346.2:c.444C=	NP_001336275.1:p.Ser148=
NM_001349347.2:c.438C=	NP_001336276.1:p.Ser146=
NM_001349348.2:c.288C=	NP_001336277.1:p.Ser96=